AVID Medical Recalls Plastic Trays Due to Lubricant Contamination
AVID Medical, Inc. is recalling 28 units of EURO053 plastic trays potentially contaminated with manufacturing lubricant. The units were distributed in AZ, CA, FL, MD, NE, and TX.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as Class II because the product may be contaminated with a lubricant, which may cause temporary or medically reversible adverse health consequences. The source does not report any illnesses, injuries, or deaths.
Plain-English summary
AVID Medical, Inc. is recalling 28 units of PLASTICS TRAY, Model/Item Number (Kit) EURO053. The recall is due to the potential contamination of the product with a lubricant used during the manufacturing process.
The affected units were distributed nationwide in the states of Arizona, California, Florida, Maryland, Nebraska, and Texas. The specific lot numbers for the recalled kits are 1674613, and the recalled supplier component is A902416 with supplier lot number NGKU3975.
The source text does not provide specific instructions for consumers or healthcare providers on how to handle the recalled product, nor does it report any illnesses, injuries, or deaths associated with the contamination.
The recalled product
- Product
- PLASTICS TRAY; Model/Item Number (Kit): EURO053;
- Manufacturer
- AVID Medical, Inc.
- Category
- Medical Device — Surgical Trays
- Hazard
- Affected units
- 28
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (5)
- Model/Item Number (Kit): EURO053
- UDI-DI: 10809160423813
- Kit Lot Numbers: 1674613
- Recalled Supplier Component (in kit): A902416
- Recalled Supplier Lot Number (in kit): NGKU3975
Distribution
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